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Recalls distributed in Louisiana

These notices name Louisiana in the distribution list the company gave its agency. That list says where the product was shipped, not where it ended up — a recalled item can travel with a shopper, and some notices list no states at all.

3,329 stored notices name Louisiana, reported between Jun 20, 2012 and Nov 11, 2026. A further 48,743 notices were distributed nationwide, so they reach Louisiana too — those are in the archive.

Medical devices

Reported Sep 23, 2026Updated Sep 29, 2026

Philips Patient Information Center iX REF:866389

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Philips North America

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 23, 2026Updated Sep 29, 2026

GM Helix Implant, REF: 109.984;

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Straumann USA LLC

FDA (openFDA device enforcement)

Medical devices

Reported Sep 23, 2026Updated Sep 29, 2026

REF:2B5ST Ethicon Endo-Surgery, Inc. XCEL BLADELESS TROCAR W/OPTIVIEW TECHNOLOGY & SLEEVE 5MM X 75MM

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Stryker Sustainability Solutions

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Sep 23, 2026Updated Sep 29, 2026

Rice & Bean Burrito. Ingredients: Rice, Refried Beans, Black Beans, Flame Roasted Corn, Pico De Gallo, Cheese. Net Wt:…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Taylor Fresh Foods Inc.

24 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Sep 23, 2026Updated Sep 29, 2026

Brand Name: HEMOSPRAY ENDOSCOPIC HEMOSTAT Product Name: HEMOSPRAY ENDOSCOPIC HEMOSTAT Model/Catalog Number: HEMO-7,…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Wilson-Cook Medical Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Sep 16, 2026Updated Sep 22, 2026

Products that contain the Pericare Wipes: Bardex Lubricath Foley Catheter Tray REF: 899914 899916 899918 UDI codes:…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

C.R. Bard Inc.

5 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 9, 2026Updated Sep 14, 2026

Brand Name: Extension Set Product Name: DISCOFIX FOUR WAY STOPCOCK Model/Catalog Number: 456025

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

B Braun Medical Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Sep 9, 2026Updated Sep 14, 2026

Baxter Novum IQ Syringe Pump, Model Number 40800BAXUS

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Baxter Healthcare Corporation

20 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 9, 2026Updated Sep 27, 2026

5008X Standard HD Pre-Flush Standard Blood Tubing Set Part Number 03-5110-6

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Fresenius Medical Care Renal Therapies Group, LLC

6 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 9, 2026Updated Sep 14, 2026

HEALON EndoCoat PRO, REF: 10300012 (US/CAN) HEALON DUET PRO II, REF: 10300016 (US/CAN) HEALON EndoCoat PRO, REF:…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Johnson & Johnson Surgical Vision, Inc.

FDA (openFDA device enforcement)

Food

Reported Sep 9, 2026Updated Sep 16, 2026

Food to Live brand Organic Supergreens mix (kale, moringa leaf, wheat grass, & spirulina), 8 oz, 1 lb, 1.5 lb, 3 lb, 6…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Lexunder Inc.

FDA (weekly enforcement report)

Food

Reported Sep 2, 2026Updated Sep 13, 2026

Byron White FORMULAS A-P Herbal Supplement 1.0 fl. oz./30 mL May Contain Nuts (Juglans nigra hull) Byron White Formulas…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Byron White Formulas, Inc.

2 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Sep 2, 2026Updated Sep 7, 2026

Outshine Fruit Bar Watermelon, 6-Count 2.5 ounce with UPC 041548413624, packaged in paper outer cartons; individual…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Dreyer's Grand Ice Cream Inc.

1 more product in this recall

FDA (openFDA food enforcement)

Food

Reported Sep 2, 2026Updated Sep 16, 2026

Outshine Fruit Bars Strawberry, 6-Count 2.5 ounce, with UPC 041548610047, packaged in paper outer cartons; individual…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Dreyer's Grand Ice Cream Inc.

3 more products in this recall

FDA (weekly enforcement report)

Food

Reported Sep 2, 2026Updated Sep 16, 2026

hodo CHILI CRISP LIGHTLY FRIED TOFU. NET WT 8oz. KEEP REFRIGERATED. Manufactured by: Hodo Inc., Oakland, CA 94608. UPC:…

Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.

Hodo Inc.

FDA (weekly enforcement report)

Medical devices

Reported Aug 26, 2026Updated Sep 7, 2026

BD Needle Kit for Powered Driver 15mm x 15Ga, REF: D015151NK, BD Needle Kit for Powered Driver 25mm x 15Ga, REF:…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Bard Access Systems, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 26, 2026Updated Sep 7, 2026

Esteem Body Soft Convex Urostomy Pouch Model/Catalog Numbers: 423703, 423704, 423705, 423707, 423708, 423709, 423710,…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

ConvaTec, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 26, 2026Updated Sep 7, 2026

EndoFLIP System that includes: ENDOFLIP 1 SYSTEM EF-100 05391530810050 10884521809307 REFURBISHED SYSTEM RFG-EF100…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Covidien, LLC

FDA (openFDA device enforcement)

Food

Reported Aug 26, 2026Updated Sep 7, 2026

Dairyland Produce, LLC Pepper Jalapeno, repackaged into the following sized clear plastic bags: 1. 1 lb., item number…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Dairyland Produce, LLC

FDA (openFDA food enforcement)

Medical devices

Reported Aug 26, 2026Updated Sep 7, 2026

Paragonix Technologies Inc. KidneyVault Portable Renal Perfusion System REF# PRGNX-8008-001

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Paragonix Technologies Inc.

FDA (openFDA device enforcement)

Food

Reported Aug 26, 2026Updated Sep 7, 2026

Prospector Popcorn Maple Walnut Ice Cream Gourmet Popcorn 3.5 oz.

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

Prospector Popcorn, LLC

3 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Aug 26, 2026Updated Sep 7, 2026

Dentsply Sirona Capsule Mixer Model No. 5546068

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

SDI Limited

FDA (openFDA device enforcement)

Food

Reported Aug 26, 2026Updated Sep 7, 2026

Whole Foods Medium Pico de Gallo Guacamole Dip, Keep Refrigerated. Packed in various sized clear plastic containers.…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

WFM Purchasing, LP

9 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Aug 19, 2026Updated Aug 25, 2026

BIOFIRE Respiratory Panel 2.1 (RP2.1) REF 423742 UDI code: 00815381020529 PCR-based multiplexed nucleic acid test, in…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

BioFire Diagnostics, LLC

FDA (openFDA device enforcement)

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Other states

RecallNow is not a government agency. Every notice above was published by the FDA, USDA FSIS or CPSC and links back to its source. Browse the whole archive.